Hydrogel from acellular porcine adipose tissue promotes survival of adipose tissue transplantation

Biomed Mater. 2021 Apr 30;16(4). doi: 10.1088/1748-605X/abf982.

Abstract

Lipofilling is a popular technique for soft tissue augmentation, limited by unpredictable graft survival. This study aimed at exploring the effect of hydrogel from acellular porcine adipose tissue (HAPA) on angiogenesis and survival of adipose tissue used for lipofilling. The effect of HAPA on adipose-derived stem cells (ADSCs) proliferation, adipogenic differentiation, and vascular endothelial growth factor (VEGF) secretion were evaluated in hypoxia and normoxiain vitro. For thein vivostudy, adipose tissue with phosphate buffered saline, ADSCs, and HAPA (with or without ADSCs) were co-injected subcutaneously into nude mice. HAPA-ADSCs mixture (tissue engineering adipose tissue) was also grafted. Gross observation, volume measurement, and ultrasound observation were assessed. For histological assessment, hematoxylin and eosin, perilipin, cluster of differentiation 31 (CD31), Ki67, and transferase-mediated d-UTP nick end labelling (TUNEL) staining were performed. HAPA improved ADSCs proliferation, VEGF secretion, and adipogenic differentiation under normoxia and hypoxia conditionsin vitrostudy. For thein vivostudy, HAPA showed improved volume retention and angiogenesis, and reduced cell apoptosis when compared to ADSCs-assisted lipofilling and pure lipofilling. In conclusion, HAPA could maintain ADSCs viability and improve cell resistant to hypoxia and might be a promising biomaterial to assist lipofilling.

Keywords: adipose derived stem cells; adipose tissue; angiogenesis; biomaterial; extracellular matrix; hypoxia; lipofilling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue* / cytology
  • Adipose Tissue* / drug effects
  • Adipose Tissue* / physiology
  • Animals
  • Cell Differentiation / drug effects
  • Cell Hypoxia
  • Decellularized Extracellular Matrix* / chemistry
  • Decellularized Extracellular Matrix* / pharmacology
  • Graft Survival / drug effects
  • Hydrogels* / chemistry
  • Hydrogels* / pharmacology
  • Male
  • Mesenchymal Stem Cell Transplantation
  • Mesenchymal Stem Cells* / drug effects
  • Mesenchymal Stem Cells* / metabolism
  • Mice
  • Mice, Nude
  • Swine
  • Tissue Engineering

Substances

  • Decellularized Extracellular Matrix
  • Hydrogels